QC Analytical Development Chemist

17h17 hours ago

Bristol Myers Squibb

Shanghai, CN · Full-time · CNY 350,000 – CNY 550,000

About this role

Working at Bristol Myers Squibb means challenging, meaningful, life-changing work that transforms patients' lives and careers. Uniquely interesting projects happen daily, from production line optimization to cell therapy breakthroughs. Thrive alongside high-achieving teams with growth opportunities of uncommon scale.

Test finished products, raw materials, packaging materials, intermediates, stability samples, and validation samples per testing standards, general methods, Pharmacopeia, and SOPs. Provide timely, accurate results and reports. Record test procedures and lab activities following SOP requirements.

Perform product validations per protocol, prepare, store, and test solutions and buffers per manuals or SOPs. Complete calibration, maintenance, and care of assigned instruments to ensure they meet analytical needs. Maintain a clean, safe laboratory environment and handle waste per SOP.

Develop new analytical methods, ensure successful method transfer to SASS, and support new product registration. Establish and revise related SOPs. Bristol Myers Squibb offers balance, flexibility, competitive benefits, and programs to pursue work and personal goals.

Empowered in a supportive culture with values of passion, innovation, urgency, accountability, inclusion, and integrity. Apply even if your resume doesn't perfectly match—transform your career through science.

Requirements

Proficiency in analytical testing of pharmaceuticals per Pharmacopeia, standards, and SOPs
Experience recording lab activities and reporting results per SOP
Knowledge of product validation protocols in QC environments
Skills in preparing, testing, and storing solutions and buffers
Ability to calibrate and maintain analytical instruments
Expertise in developing new analytical methods for QC
Familiarity with method transfer processes in pharmaceutical labs
Understanding of GMP lab safety, waste handling, and clean environments

Responsibilities

Test finished product, raw material, packing material, intermediate, stability sample and validation sample according to testing standard, general method, Pharmacopeia, etc., and provide timely and accurate results and report timely
Record test procedure and lab activity, report test results following SOP
Finish the validation of product according to the protocol
Prepare, store and test solution and buffer solution following manual or SOP
Accomplish the calibration and maintenance of assigned instruments to ensure they are in good order to meet analytical needs
Develop new analytical methods
Ensure successful method transfer to SASS and support registration work of new products
Establish and revise related SOPs